Achieving the highest diagnostic yield possible with phenotype-based prioritization of variants

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Why a diagnosis is so important for rare disease patients

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David Atkins joins the National Genomics Board as BIA representative

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Congenica Enters Cancer Collaboration with University of Glasgow Spinout Gabriel Precision Oncology

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Webinar on Demand: Enabling Genomic Medicine

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Congenica Contributes to Key Priority within UK Rare Disease Framework

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Webinar on Demand: The role of automated classification in clinical rare disease reporting

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Congenica Launches Patient Advocacy and Engagement Advisory Board

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Congenica Local Cloud Solution to Enable High-quality, Scalable Genomic Analysis in China

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2020 – The Year of Healthcare Heroes and International Teamwork

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Congenica v3.0 - Overcoming Challenges to Accelerate Variant Classification

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Achieving the highest diagnostic yield possible with phenotype-based prioritization of variants

Read More

Why a diagnosis is so important for rare disease patients

Read More

David Atkins joins the National Genomics Board as BIA representative

Read More

Congenica Enters Cancer Collaboration with University of Glasgow Spinout Gabriel Precision Oncology

Read More

Webinar on Demand: Enabling Genomic Medicine

Read More

Congenica Contributes to Key Priority within UK Rare Disease Framework

Read More

Webinar on Demand: The role of automated classification in clinical rare disease reporting

Read More

Congenica Launches Patient Advocacy and Engagement Advisory Board

Read More

Congenica Local Cloud Solution to Enable High-quality, Scalable Genomic Analysis in China

Read More

2020 – The Year of Healthcare Heroes and International Teamwork

Read More

Congenica v3.0 - Overcoming Challenges to Accelerate Variant Classification

Read More